Access the full text.
Sign up today, get DeepDyve free for 14 days.
M. Greene, B. Benacerraf, F. Frigoletto (1987)
Reliable criteria for the prenatal sonographic diagnosis of alobar holoprosencephaly.American journal of obstetrics and gynecology, 156 3
E Roach, W DeMyer, K Palmer, M Conneally, AD Merritt (1975)
Malformation syndromes. Papers presented at the Johns Hopkins Hospita, XI
F. Probst, A. Brun, I. Castroviejo (1979)
The Prosencephalies: Morphology, Neuroradiological Appearances and Differential Diagnosis
R. Benawra, H. Mangurten, D. Duffell (1980)
Cyclopia and other anomalies following maternal ingestion of salicylates.The Journal of pediatrics, 96 6
Kara Mayden, M. Tortora, Richard Berkowitz, Michael Bracken, John Hobbins (1982)
Orbital diameters: a new parameter for prenatal diagnosis and dating.American journal of obstetrics and gynecology, 144 3
S. Schwartz, J. Meekins, S. Panny, Chen-Chih Sun, Maimon Cohen, John Opitz (1983)
Cebocephaly‐holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX,del(7)(pter→q32:)]American Journal of Medical Genetics, 15
R. Filly, D. Chinn, P. Callen (1984)
Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.Radiology, 151 2
A. Schinzel, J. Opitz, J. Reynolds (1986)
A further case of cyclopia due to unbalanced segregation of a previously reported rcp(1;7)(q32;q34) familial translocation.American journal of medical genetics, 24 1
R. Schnabel, S. Hansen (1983)
Karyotype 47, XXY,18p‐ in a newborn child with holoprosencephalyClinical Genetics, 23
KK Sulik, MC Johnston (1982)
Embryonic origin of holoprosencephaly: Inteerrelationship of the developing brain and face, 1
H. Patel, C. Dolman, M. Byrne (1972)
Holoprosencephaly with median cleft lip. Clinical, pathological, and echoencephalographic study.American journal of diseases of children, 124 2
E. Jaxies, G. Leeuwen (1970)
Familial CebocephalyClinical Pediatrics, 9
N Ben‐Hur, H Ashur, M Murreri (1978)
An unusual case of median cleft lip with orbital hypotelorism: A missing link in the classification, 15
L. Holmes, S. Driscoll, L. Atkins (1974)
Genetic Heterogeneity of CebocephalyJournal of Medical Genetics, 11
D. Blackwell, J. Spinnato, G. Hirsch, H. Giles, J. Sackler (1982)
Antenatal ultrasound diagnosis of holoprosencephaly: a case report.American journal of obstetrics and gynecology, 143 7
GM Ronen, WL Andrews (1988)
Holoprosencephaly as a possible embryonic alcohol effect, 23
MM Cohen, J Jirasek, RT Guzman, RJ Gorlin, MQ Peterson (1971)
The Clinical Delineation of Birth Defects, VII
G. Pilu, R. Romero, N. Rizzo, P. Jeanty, L. Bovicelli, J. Hobbins (1987)
Criteria for the Prenatal Diagnosis of HoloprosencephalyAmerican Journal of Perinatology, 4
E. Ives, C. Houston (1980)
Autosomal recessive microcephaly and micromelia in Cree Indians.American journal of medical genetics, 7 3
H Hattori, T Okuno, T Momoi, K Kataoka, H Mikawa, K Shiota (1987)
Brief clinical report: Single central maxillary incisor and holoprosencephaly, 28
C. Romshe (1973)
Hypothalamic-pituitary dysfunction in siblings of patients with holoprosencephalyThe Journal of Pediatrics, 83
John Opitz (1982)
The developmental field concept in clinical genetics.The Journal of pediatrics, 101 5
M. Barr, J. Hanson, K. Currey, S. Sharp, H. Toriello, R. Schmickel, Golder Wilson (1983)
Holoprosencephaly in infants of diabetic mothers.The Journal of pediatrics, 102 4
ML Begleiter, DJ Harris (1980)
Brief clinical report: Holoprosencephaly and endocrine dysgenesis in brothers, 7
R. Hintz, R. Hintz, Manfred Menking, Manfred Menking, Juan Sotos, Juan Sotos (1968)
Familial holoprosencephaly with endocrine dysgenesis.The Journal of pediatrics, 72 1
G. Gimelli, C. Cuoco, M. Lituania, M. Cordone, M. Aricò, E. Bianchi, P. Maraschio, O. Zuffardi (1985)
Dup(3)(p2----pter) in two families, including one infant with cyclopia.American journal of medical genetics, 20 2
RD Smart, J Ross, G Amann, MM Nelson (1986)
Brief clinical report: Cyclopia as a result of an unbalanced familial translocation, rep (7;18) (q34;q21), 24
Van Dyke, Dl, W. L., Logan M, Pai Gs, Golder Wilson, J. Lambert, P. Philip, G. Charpentier, M. Ferrari, M. Donzeau, N. Ayraud (1984)
Triploidy with cyclopia and identical HLA alleles in the parents.Journal of Medical Genetics, 21
E. Saunders, D. Shortland, P. Dunn, From (1984)
What is the incidence of holoprosencephaly?Journal of Medical Genetics, 21
M. Begleiter, D. Harris (1980)
Holoprosencephaly and endocrine dysgenesis in brothers.American journal of medical genetics, 7 3
IW Lurie, IA Korotkova, DV Zaletaje, LI Smirnova, LV Podlechshuk, DB Gurevich (1987)
Trisomy for the distal part of the short arm of chromosome 3, 41
E James, G VanLeeuwen (1970)
Familial cebocephaly, case description and survey of the anomaly, 9
A Schinzel (1983)
Catalogue of Unbalanced Chromosome Aberrations in Man
H. Hattori, T. Okuno, T. Momoi, K. Kataoka, Haruki Mikawa, Kohei Shiota, J. Opitz, J. Reynolds (1987)
Single central maxillary incisor and holoprosencephaly.American journal of medical genetics, 30 4
Alice Martin, J. Perrin, W. Muir, E. Ruch, I. Schafer (1977)
An autosomal dominant midline cleft syndrome resembling familial holoprosencephalyClinical Genetics, 12
F. Chervenak, G. Isaacson, M. Mahoney, M. Tortora, T. Mesologites, J. Hobbins (1984)
The obstetric significance of holoprosencephaly.Obstetrics and gynecology, 63 1
MM Cohen, RJ Gorlin (1969)
The Clinical Delineation of Birth Defects: Part II, Malformation Syndromes, V
T. Baranowski, Y. Tsong, J. Henske, J. Dunn, P. Hooks (1988)
Ethnic Variation in Blood Pressure among Preadolescent ChildrenPediatric Research, 23
S. Berry, M. Pierpont, R. Gorlin (1984)
Single central incisor in familial holoprosencephaly.The Journal of pediatrics, 104 6
A. Schinzel, John Opitz (1984)
Cyclopia and cebocephaly in two newborn infants with unbalanced segregation of a familial translocation rcp (1;7)(q32;q34).American journal of medical genetics, 18 1
L. Deligdisch, C. Legum, M. Peyser, R. Toaff (1978)
Cyclopia associated with triploidy and hydatidiform mole: a case report.Teratology, 18 2
JM Opitz (1985)
Editorial comment: The developmental field concept, 21
P. Pfitzer, H. Müntefering (1968)
Cyclopism as a Hereditary MalformationNature, 217
Maximilian Münke, Maximilian Münke, Beverly Emanuel, E. Zackai (1988)
Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature.American journal of medical genetics, 30 4
S Schwartz, J Meekins, SR Panny, C‐CJ Sun, MM Cohen (1983)
Brief clinical report: Cebocephaly‐holoprosencephaly in a newborn girl with a terminal 7q deletion [46,XX del(7) (pter → q32:)], 15
B. Benacerraf, F. Frigoletto, F. Bieber (1984)
The fetal face: ultrasound examination.Radiology, 153 2
CR Fitz (1983)
Holoprosencephaly and related entities, 25
G. Isaacson, J. Hobbins, U. Chitkara, M. Tortora, R. Berkowitz (1985)
Diagnosis and Management of Fetal HoloprosencephalyObstetrics & Gynecology, 66
J. Opitz, J. Reynolds (1985)
The developmental field concept.American journal of medical genetics, 21 1
JM Cantú, R Fragoso, D Garcia‐Cruz, J Sanchez‐Corona (1978)
Annual Review of Birth Defects, 1977: Recent Advances and New Syndromes, XIV
JP Fryns, H Van den Berghe (1988)
Letter to the Editor: Single central maxillary incisor and holoprosencephaly, 30
M. Agapitos, M. Georgiou-Theodoropoulou, A. Koutselinis, N. Papacharalampus (1986)
Cyclopia and maternal ingestion of salicylates.Pediatric pathology, 6 2-3
M. Stabile, A. Bianco, S. Iannuzzi, M. Buonocore, V. Ventruto (1985)
A case of suspected teratogenic holoprosencephaly.Journal of Medical Genetics, 22
PD Cayea, I Balcar, O Alberti, TB Jones (1984)
Prenatal diagnosis of semilobar holoprosencephaly, 142
N. Martin, B. Steinberg, J. Opitz (1983)
The dup(3)(p25 → pter) syndrome: A case with holoprosencephalyAmerican Journal of Medical Genetics, 14
SK Ludwin, N Malamud (1977)
Radiology of the Skull and Brain
E. Gilbert, J. Opitz (1976)
The pathology of some malformations and hereditary diseases of the respiratory tract.Birth defects original article series, 12 6
Ronald Smart, Judy Ross, Gabriel Amann, Matilda Nelson, James Reynolds (1986)
Cyclopia as a result of an unbalanced familial translocation, rcp(7;18)(q34;q21)American journal of medical genetics, 24 2
W. Demyer, W. Zeman, C. Palmer (1964)
THE FACE PREDICTS THE BRAIN: DIAGNOSTIC SIGNIFICANCE OF MEDIAN FACIAL ANOMALIES FOR HOLOPROSENCEPHALY (ARHINENCEPHALY).Pediatrics, 34
Benke Pj, Cohen Mm (1983)
Recurrence of holoprosencephaly in families with a positive history.Clinical Genetics, 24
Y. Gillerot, J. Hustin, L. Koulischer, V. Viteux (1987)
Prenatal diagnosis of a dup(3p) with holoprosencephaly.American journal of medical genetics, 26 1
EF Gilbert, JM Opitz (1976)
Growth Problems and Clinical Advances, XII
Holoprosencephaly refers to a spectrum of craniofacial malformations including cyclopia, ethmocephaly, cebocephaly, and premaxillary agenesis. Etiologic heterogeneity is well documented. Chromosomal, genetic, and teratogenic factors have been implicated. Recognition of holoprosencephaly as a developmental field defect stresses the importance of close scrutiny of relatives for mild forms such as single median incisor, hyptelorism, bifid uvula, of potuitary deficiency.
American Journal of Medical Genetics Part A – Wiley
Published: Oct 1, 1989
Keywords: ; ;
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.